Abstract
Background
Infections caused by Acinetobacter baumannii are becoming a rising public health problem due to its high degree of acquired and intrinsic resistance mechanisms. Bacterial lipases penetrate and damage host tissues, resulting in multiple infections. Because there are very few effective inhibitors of bacterial lipases, new alternatives for treating A. baumannii infections are urgently needed. In recent years, Brassica vegetables have received a lot of attention since their phytochemical compounds have been directly linked to diverse antimicrobial actions by inhibiting the growth of various Gram-positive and Gram-negative bacteria, yeast, and fungi. Despite their longstanding antibacterial history, there is currently a lack of scientific evidence to support their role in the management of infections caused by the nosocomial bacterium, A. baumannii. This study aimed to address this gap in knowledge by examining the antibacterial and lipase inhibitory effects of six commonly consumed Brassica greens, Chinese cabbage (CC), curly and Tuscan kale (CK and TK), red and green Pak choi (RP and GP), and Brussels sprouts (BR), against A. baumannii in relation to their chemical profiles.
Methods
The secondary metabolites of the six extracts were identified using LC-QTOF-MS/MS analysis, and they were subsequently correlated with the lipase inhibitory activity using multivariate data analysis and molecular docking.
Results
In total, 99 metabolites from various chemical classes were identified in the extracts. Hierarchical cluster analysis (HCA) and principal component analysis (PCA) revealed the chemical similarities and variabilities among the specimens, with glucosinolates and phenolic compounds being the major metabolites. RP and GP showed the highest antibacterial activity against A. baumannii, followed by CK. Additionally, four species showed a significant effect on the bacterial growth curves and demonstrated relevant inhibition of A. baumannii lipolytic activity. CK showed the greatest inhibition (26%), followed by RP (21%), GP (21%), and TK (15%). Orthogonal partial least squares-discriminant analysis (OPLS-DA) pinpointed 9 metabolites positively correlated with the observed bioactivities. Further, the biomarkers displayed good binding affinities towards lipase active sites ranging from −70.61 to −30.91 kcal/mol, compared to orlistat.
Conclusion
This study emphasizes the significance of Brassica vegetables as a novel natural source of potential inhibitors of lipase from A. baumannii.
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Background
Brassicaceae is made up of 350 genera, including Camelina, Crambe, Sinapis, Thlaspi, and Brassica, which have over 3,500 species. Brassica is the most important genus, encompassing crops and species of great worldwide economic value such as cabbage, cauliflower, and broccoli. Brassica crops have sparked scientific interest due to their potential applications in treating various cardiovascular ailments and gastrointestinal cancers [1]. Additionally, the antioxidant capacity and antibacterial activity of several Brassica vegetables, such as kale, Brussels sprouts, cabbage, broccoli, and radish have been previously studied [2,3,4,5].
Sulfur-containing compounds, glucosinolates, are the main identified compounds in Brassica vegetables and they are responsible for their characteristic aroma [6] and various biological activities [7]. Several studies have also reported the existence of polyphenolics as major constituents in Brassica leaves [8, 9]. The most commonly reported flavonoids are quercetin, kaempferol, and isorhamnetin, which are glycosylated and/or acylated with one or more hydroxycinnamic acids, including coumaric, caffeic, sinapic, and ferulic acids [8, 10]. Several reports correlated the high polyphenolic content of Brassica leaves to their antioxidant, anticancer, antihyperglycemic, and hepatoprotective potential [11,12,13,14]. The bioactive potential of Brassicaceae glucosinolates and isothiocyanates is obvious, making them great candidates for biocontrol of pathogens that cause severe illnesses in humans [15]. They may have inhibitory activity against a wide range of microorganisms, including fungi and pathogenic bacteria like Escherichia, Salmonella, Bacillus, Staphylococcus, Klebsiella, and Listeria, or in synergism with conventional antibiotics to enhance their effectiveness [15, 16]. Other studies found that isothiocyanates derived from B. campestris ssp. pekinensis and B. rapa var. rapa, such as benzyl, 3-butenyl, and 2-phenyl ethyl isothiocyanate had stronger antibacterial effects against Gram-positive bacteria than Gram-negative bacteria when tested using the agar disc diffusion assay [17]. Furthermore, the antibacterial and antioxidant activities of several Brassica phenolics were previously discussed [3, 9]. Different flavonoids in cabbage, such as genistein, kaempferol, naringenin, and catechin revealed potent antibacterial activity against the Staphylococcus aureus and Escherichia coli [9].
Metabolomics aims at the identification and quantification of small molecules in biological samples, such as plant materials [18]. Recently, LC-MS/MS has gained popularity as the preferred platform for metabolomic studies due to its high throughput, mass accuracy, resolution, detailed characterization, and broad coverage of metabolites [19]. LC-MS/MS metabolomics analyses are combined with multivariate analysis methods, in particular, principal component analysis (PCA) and orthogonal partial least squares-discriminant analysis (OPLS-DA) to uncover chemical variations among groups of samples, providing an effective route for the subsequent identification of bioactive components [20, 21]. Nevertheless, previous research on Brassica species has focused on targeting specific classes of constituents, such as polyphenolic compounds [8, 10, 22] or glucosinolates [23,24,25]. In our study, we apply this LC-MS/MS-based metabolomics approach to obtain comprehensive profiles of both secondary and primary metabolites in these economically valuable vegetables. Moreover, to add a biological dimension to our findings, the antibacterial activity of the selected Brassica species was evaluated against Acinetobacter baumannii. This Gram-negative pathogen is notorious for its impact on vulnerable intensive care unit patients, leading to severe infections such as ventilator-associated pneumonia and bacteremia. These infections pose a significant threat in developing countries [26]. A. baumannii is an emerging pathogen that currently holds the top position on the World Health Organization (WHO) list of pathogens in urgent need of new effective antibacterial agents [27]. Unfortunately, the treatment of A. baumannii is often complicated due to its inherent resistance to many commonly used antibiotics, as well as its ability to become resistant to numerous others. This resulted in significant outbreaks of multi-drug resistance (MDR) strains, including resistance to last-resort antibiotics such as colistin and tigecycline [28]. As far as the authors know, the antibacterial and anti-virulence activity of Brassica leaves against A. baumannii remains unexplored.
Molecular docking serves as a valuable tool in drug discovery programs, especially for natural products, by predicting interactions of small molecules with drug targets [29]. This process guides synthesis decisions, aids in understanding some traditional medicinal plant applications, and identifies new ones. Moreover, it reduces the effort required to isolate active compounds for structure elucidation studies and minimizes the need for bioactivity assessments, which are significant challenges in developing countries [29, 30, 31]. In summary, this study emphasizes the importance of Brassica greens as a natural source of antibacterial and anti-virulence compounds with potential implications for the food and nutraceutical industries.
This study presents the first comparative untargeted metabolomics approach, utilizing liquid chromatography-quadrupole time-of-flight tandem mass spectrometry (LC-QTOF/MS/MS) combined with multiple chemometrics tools, for correlating the chemical profiles of Brassica greens, including Chinese cabbage (CC), Curly (CK) and Tuscan kale (TK), green (GP), red Pak choi (RP), and Brussels sprouts (BR) to their antibacterial and lipolytic activities against A. baumannii. The findings were further validated using molecular docking to predict possible binding conformations of the different biomarkers with A. baumannii lipase active sites and to unravel the mode of interactions underlying the predicted lipolytic inhibitory effects of Brassica phytochemicals for the first time.
Materials and methods
Plant material
Six Brassica species were supplied by Makar Farm (Giza, Egypt) in March 2021 and kindly identified by Prof. Dr. Abdel-Halim Mohammed (Professor of Agriculture, Flora department, Agricultural Museum, Dokki, Giza, Egypt). Samples were kept in the Museum of Pharmacognosy Department, Faculty of Pharmacy, Cairo University. Voucher specimen numbers were 06032021I for Brassica rapa ssp. chinensis (Chinese cabbage (CC)), 07032021X for B. olearacea var. Sabellica (curly kale (CK)), 06032021II for B. olearaceae var. palmifolia (Tuscan kale (TK)), 07032021 IV for B. rapa ssp. pekinensis (green Pak choi (GP) and red Pak choi (RP)), and 07032021 VIII for B. olearaceae var. gemmifera (Brussels sprouts (BR)).
Plant material extraction
Forty grams of the air-dried leaves of each Brassica species were extracted three times with one liter of methanol assisting by sonication. Each extract was then dried under vacuum in a rotary evaporator at 50 ºC and the residue was kept in a tight container until analysis. Each sample species was prepared as three biological replicates under the same conditions. Samples for LC-QTOF-MS/MS were prepared by dissolving 10 mg of each extract in 1 mL of methanol followed by centrifugation at 13,250 g for 10 min at 25 ºC and filtration through 0.22 nm syringe filter.
LC-QTOF-MS/MS analysis
All LC-QTOF-MS/MS experiments were performed in a 1260 Infinity liquid chromatograph coupled to a 6546 LC/QTOF mass spectrometer with an orthogonal electrospray ionization (ESI) interface (Agilent Technologies, Waldron, Germany). Acetonitrile (ACN), water, methanol (LC-MS grade), and formic acid (≥ 95.0%) were supplied by Merck (Darmstadt, Germany). The chromatographic separation and MS detection conditions were reported in our previous work [20, 21].
Identification of the detected metabolites was achieved based on the exact mass, MS/MS fragmentation pattern, and molecular formula along with the current literature. The raw LC-QTOF-MS/MS data was converted with ProteoWizard 3.0 (www.proteowizard.org) into mzXML format and processed using MZmine 2.53 software (https://github.com/mzmine/mzmine2/releases/tag/v2.53) [32]. The obtained peak lists (3697 detected compounds) were then aligned and subjected to formula prediction and identification using LipidMaps (https://www.lipidmaps.org/), KEGG (https://www.kegg.jp/kegg/compound/), and MS/MS fragmentation patterns (99 identified metabolites). The data of the identified metabolites was then converted into a CSV file, containing the ID number (ID), retention time (tr), m/z, peak intensity, molecular formula, and metabolite identity in the different samples. The data set with the intensity information (18 columns: 6 Brassica species x 3 replicates) and 3697 rows (detected compounds) was then mean-centered, and exported to SIMCA Version 14 (Umetrics, Umeå, Sweden), for further analysis using hierarchical cluster analysis (HCA), principal component analysis (PCA), and orthogonal partial least squares-discriminant analysis (OPLS-DA).
Microbiological analysis
Determination of the minimum inhibitory concentration (MIC)
The minimum inhibitory concentration (MIC) of extracts against the multidrug-resistant (MDR) A. baumannii strain AB5075 was determined using the microdilution method, following established protocols [33, 34]. Extracts were dissolved in DMSO and serially diluted in saline to calibrate in the concentration range between 1024 µg/mL and 0.5 µg/mL. A. baumannii cultures were grown to the mid-logarithmic phase, adjusted to a standardized density (0.5 McFarland’s standard), and exposed to the extracts in 96-well microtiter plates. Bacterial growth was assessed after 24 h incubation, and the MIC was defined as the lowest extract concentration that prevented visible growth. Orlistat served as a control.
Determination of the effective killing concentration
To determine the effective killing concentration of the orlistat and the studied extracts, especially those that showed turbidity with MHB, the assay described by the WHO [27] was adopted. The principle of this assay is that tetrazolium salts can form highly colored products upon reduction by viable biological systems. In the case of 2, 3, and 5-triphenyl tetrazolium (TTC), it is reduced to red tri-phenyl-formazan. Accordingly, the effective killing concentration can be considered as the lowest concentration that prevents the production of red tri-phenyl-formazan [35]. Briefly, the bacterial inoculum was prepared as described above for the MIC determination. Then, 15 µL aliquots corresponding to ∼ 5 × 105 CFU were added to each well in a 96-well U-shaped microtiter plate. Then 150 µL of MHB with the tested extract was added to give a final extract concentration ranging from 420 µg/mL to 640 µg/mL, followed by incubation for 18 h at 37 °C. Positive and negative controls were included as described before for MIC experiments. Then, a 0.5% (m/v) solution of TTC (Sigma-Aldrich) was added to all the wells at a final concentration of 10% (v/v) and then incubated for 2 h at 37 °C. Finally, the wells that showed red color formation indicated the presence of viable cells.
Growth curves
The in vitro growth extent and rate of A. baumannii in the presence of the studied extracts were evaluated by establishing growth curves [36]. Briefly, the OD of an overnight bacterial culture was adjusted at OD600 ∼ 0.5 and then diluted to 1:100 (v/v) in fresh LB. The culture was then separately mixed with the extracts to a final concentration of 512 µg/mL for both BR and CC and 256 µg/mL for the other 4 species. DMSO was also included as a control in equivalent amounts as in the extract. Cultures were incubated at 37 °C while shaking at 180 rpm. Aliquots from each culture were withdrawn and their OD600 were measured every hour for 10 h and finally after 24 h. Measurements were used for the construction of growth curves by plotting OD600 values versus time.
Lipolytic activity assay
Lipolytic activity assay was conducted according to the method described by Martínez and co-workers [37] with some modifications. A. baumannii was grown to the mid-logarithmic phase (OD600 ∼ 0.6). The adjusted cultures were supplemented with the studied extracts and then mixed with an equal volume of the substrate solution. The latter consisted of 2 mM p-nitrophenyl palmitate (pNPP) (Sigma-Aldrich) in 50 mM Tris-HCl (pH 7.2, Sigma-Aldrich) containing 2% ACN (Sigma-Aldrich). The final concentration of the extracts in the assay mixture was 512 µg/mL for both BR and CC and 256 µg/mL for the other 4 species. An aliquot of the reaction mixture was transferred to a flat-bottomed 96-well plate and the p-nitrophenol (pNP) released after pNPP hydrolysis was determined by measuring the absorbance at 410 nm both at time zero and after 3 h of incubation at 37 °C. Samples incubated with the equivalent amounts of DMSO were used as controls.
Molecular docking
The identified biomarkers were subjected to molecular docking to recognize their binding modes and free energies of binding towards A. baumannii lipase receptors. The crystallographic structure of A. baumannii lipase was retrieved from Protein Data Bank (PDB ID: 5L2F). Docking analysis was performed using the AutoDock program [38]. AutoDock is a freely available suite of automated docking tools, which allows flexible ligand docking (http://autodock.scripps.edu). The 2D chemical structures of the investigated compounds and co-crystalized ligands were sketched using ChemBioDraw Ultra 14.0. To assess the efficacy of the docking method, we performed molecular redocking of co-crystalized ligands, which were validated by getting low root mean square deviation (RMSD) values between the docked and X-ray structures. Then, the co-crystalized ligand and the tested compounds were docked using the default protocol parameters. The docking results from the AutoDock program were further analyzed and visualized using Pymol software to investigate the putative interaction mechanism.
Results and discussion
Metabolite identification by LC-QTOF-MS/MS
The six Brassica leaf extracts were analyzed using LC-QTOF-MS/MS in negative ESI mode to obtain comprehensive, characteristic, and detailed metabolic fingerprints of the different species. Supplementary Fig. S1 shows representative full-scan MS base peak chromatograms for the six species. A total of 99 compounds were tentatively identified based on the exact mass, MS/MS fragmentation pattern, and molecular formula along with the current literature. The identified metabolites belonged to five chemical classes (glucosinolates, isothiocyanates, phenolic acids, flavonoids, organic, and fatty acids). A list of the identified metabolites, including the ID, Rt, m/z of the detected molecular ion and errors (< 6.2 ppm), molecular formula, and MS/MS fragments are given in Table S1. The fragmentation patterns of selected identified metabolites are displayed in the supplementary material (Figs. S2–S11).
Glucosinolates (GSL)
GSL are amino acid-derived compounds with an O-sulfated thiohydroximate attached to a β-D-glucopyranoside moiety through a thio-link [39, 40]. Based on the nature of the parent amino acid, GSL can be classified into three groups: aliphatic, indole, and aromatic GSL [40]. They are mainly present in plants of order Brassicales, in particular family Brassicaceae [41]. Fifteen GSL were identified across the six studied Brassica species, including eleven aliphatic GSL (IDs 1, 2, 3, 4, 6, 7, 8, 9, 10, 11, and 14), three indole GSLs (IDs 12, 13, and 15), and one aromatic GSL (ID 5) (Table S1 and Fig. S1).
The identified GSLs were eluted in the first seven minutes of the chromatographic run. Simple aliphatic GSL as sinigrin (ID 1) (Fig. S2), progoitrin (ID 3), and gluconapin (ID 9) exhibited the deprotonated molecular ions [M-H]− at m/z 358.0269, 388.0381, and 372.0433, respectively. They produced characteristic ion peaks at m/z 259 corresponding to thioglucosyl [C6H11O9S]– moiety, and m/z 96 corresponding to the hydrogen sulfate [HSO4]– moiety [20]. Furthermore, glucobrassicanapin (ID 11) exhibited a deprotonated molecular ion at m/z 386.0588, fragment ions at m/z 306 [M-H-SO3]−, 274 [C6H10O8S2]−, 259 [C6H11O9S]–, 95 [SO4]–, and 74 [OH-N=C=S]– (Fig. S3).
Regarding indole GSL, 4-hydroxy glucobrassicin (ID 12), glucobrassicin (ID 13), and neoglucobrassicin (ID 15) were identified in the extracts (Table S1). They exhibited the deprotonated molecular ions [M-H]− at m/z 463.0495, 447.0545, and 477.0652, respectively. MS-MS spectrum of glucobrassicin (ID 13) showed characteristic fragments at m/z 205 [M-Glc-SO3]− and 252 [M-SGlc]−. The molecular ions of IDs 15 and 12 were 30 and 16 m/z units higher than that of peak 13, denoting the presence of an extra methoxy and a hydroxy group, respectively. Therefore, they were identified as neoglucobrassicin and 4-hydroxyglucobrassicin.
Isothiocyanates
Four isothiocyanates were identified in the first four minutes of the chromatographic run (Table S1 and Fig. S1). IDs 16, 17, 18, and 19 were assigned to methiin, erucin, sulforaphane, and 1-isothiocyanato-7-(methylsulfinyl) heptane, respectively. Methiin was previously reported in B. oleracea var. capitata in cauliflower, mustard, broccoli, and turnip [42, 43]. Erucin and sulforaphane were found in broccoli [44], while 1-isothiocyanato-7-(methylsulfinyl)heptane was present in cabbage, cauliflower, kale, and broccoli [45, 46].
Phenolic acids
Twenty-six phenolic acids and their derivatives were identified in the different extracts (from ID 20 to 45, Table S1 and Fig. S1). For instance, IDs 20, 21, 24, 27, 28, and 39 were simple phenolic acids assigned to salicylic, cinnamic, caffeic, ferulic, chlorogenic, and sinapic acids, respectively. Ferulic acid (ID 27, m/z 193.0507) was present as glycoside in IDs 31, 33, 34, and 41, as well as conjugated with sinapic acid glycosides in IDs 35, 36, 43, and 45. The MS-MS spectra of ferulic acid and some of its derivatives were characterized by the presence of fragment ions at m/z 178 and 134 indicating the sequential loss of methyl and CO2 groups. Similarly, p-coumaric acid glucoside (ID 26) exhibited a deprotonated molecular ion at m/z 325.0926 and fragment ions at m/z 163 and 119 due to the successive loss of a glucose moiety and a CO2 group [20]. Moreover, chlorogenic acid (ID 28) (Fig. S4) showed a deprotonated molecular ion peak at m/z 353.0880 and fragment ions indicating the quinic acid and caffeic acid moieties at m/z 191 and 179, respectively, as well as quinic acid and caffeic acid after loss of a CO2 group at m/z 161 and 135, respectively [47].
Several hydroxycinnamoyl gentiobioses have been previously reported in brassica vegetables [48]. For example, sinapoyl hydroxy feruloyl gentiobioside (ID 36, Fig. S5) exhibited a molecular ion at m/z 739.2081 and a fragment ion at m/z 415 due to the loss of a gentiobiose moiety [(M-H)-324]–. It also showed fragment ions due to sinapic acid fragmentation (m/z 223 [sinapic acid-H]–, 205 [sinapic acid-H-H2O]–, and 164 [sinapic acid-H-CH3-CO2]–), as well as hydroxy ferulic acid fragmentation (m/z 209 and 191). Regarding IDs 43 and 45, the parent ions were observed at m/z 723.2129 and m/z 929.2733, respectively. Both showed a fragment ion due to the loss of a dihexose unit from the parent ion (i.e., 399 and 605 m/z, respectively), besides characteristic fragment ions of sinapic acid and ferulic acid (m/z 193 [ferulic acid-H]–, 175 [ferulic acid-H-H2O]–). Therefore, they were assigned as feruloyl sinapoyl gentiobioside (ID 43, Fig. S6), and feruloyl disinapoyl gentiobioside, respectively (ID 45).
Flavonoids
A total number of 22 flavonoids, from ID 46 to ID 67, were identified in the tr range between 6.5 and 9 min of the chromatographic run in the different extracts (Table S1 and Fig. S1). In agreement with the reported data [8, 10, 22, 48, 49], flavonols were the main flavonoids found in the extracts, among them 13 kaempferol, 6 quercetin, and 2 isorhamnetin derivatives, along with one flavanone (hesperetin glucoside). They were mostly present as mono-, di-, tri-, tetra-, and penta-O-glycosides limited mostly to glucosides and few rhamnosides [50]. O-acylated flavonols with hydroxycinnamic acids (caffeic, sinapic, and ferulic acids) were also identified. The sugar types could be identified by the sequential elimination of pentosyl (-132 m/z), rhamnosyl (-146 m/z), and hexosyl (-162 m/z) moieties. The identified flavonol glycosides were mainly of sophoroside type, as previously reported for the genus Brassica, which is characterized by the fragment ions corresponding to (-120 m/z) and (-180 m/z). Twelve non-acylated glycosides were identified among them six kaempferol glycosides in IDs 47, 49, 54, 63, 64, and 66. Fig. S7 shows the MS/MS spectrum of kaempferol-3-O-rhamnosyl-7-O-hexoside (ID 63) with [M-H]– at m/z 593.1509 and fragment ions at m/z 446 resulting from the elimination of rhamnosyl radical via hemolytic cleavage of the 3-O-glycosidic bond and at m/z 431 generated by the loss of a hexose at 7-position (-162 m/z). Four quercetin glycosides were identified in IDs 48, 50, 53, and 65. While two isorhamnetin glycosides were in IDs 51 and 60. Fig. S8 shows the MS/MS spectrum of brassicoside (ID 51), which showed [M-H]– at m/z 801.2087 m/z, and fragment ions at m/z 639, 476, and 315 indicating the successive loss of three glucosyl units, with the final fragment denoting the isorhamnetin aglycone ion.
Moreover, seven acylated kaempferol glycosides were identified as shown in IDs 56, 57, 58, 59, 61, 62, and 67, as well as one acylated quercetin glucoside in ID 55 that was assigned to quercetin 3-O-(2-feruloyl sophoroside)-7-O-glucoside. The MS/MS spectrum of this metabolite (ID 55, Fig. S9) showed the molecular ion [M − H]− at m/z 963.2396 and three major fragment ions, at m/z 787 [M-H-feruloyl]−, 625 [M-H-feruloyl-Glc]−, and 462 [M-H-feruloyl-2Glc]− indicated the successive loss of one feruloyl moiety followed by two glucosyl residues. While, kaempferol 3-(2-caffeoyl sophoroside)-7-O-glucoside (ID 56, Fig. S10) displayed [M-H]− at m/z 933.2307 and fragment ions due to successive loss of glucosyl residues, together with fragment ions at m/z 179 and 161 due to caffeic acid and caffeoyl radical, respectively [8, 48]. A similar fragmentation pattern was also found in kaempferol-3-O-sinapoyl sophorotrioside-7-O-glucoside (ID 57, Fig. S11), that exhibited fragment ions due to successive loss of glucosyl moieties (-162 m/z at m/z 977), sinapoyl (-206 m/z at m/z 771), and at m/z 447 corresponded to the loss of sinapoyl and 3 glucosyl moieties, as well as those produced by the inter-glycosidic bond of the sophorotrioside moiety fragmentation at m/z 753 and 591 or the characteristic ions of sinapic acid.
Organic and fatty acids
Seven organic acids were identified as fumaric (ID 68), malic (ID 69), citric (ID 70), succinic (ID 71), methyl citric (ID 72), quinic (ID 73), and shikimic acids (ID 75) (Table S1 and Fig. S1) and were previously reported in B. oleracea L. var. costata [49]. Most of the fatty acids were eluted from 8 to 20 min of the chromatographic run. In agreement with the literature [51], a total of 15 long chain mono-, di-, tri-, and polyunsaturated fatty acids (IDs 74, 76–99) were identified. For example, the [M-H]− ions of IDs 89 and 90 differed in 2 m/z units (295.2276 vs. 297.2433 m/z), hence denoting an extra double bond, as found in hydroxy octadecadienoic acid (ID 89) compared to hydroxy oleic acid (ID 90).
MIC and EIC of the extracts against A. baumannii and the effect of sub-inhibitory concentrations on growth curves
The antibacterial activity of the six leaf extracts was evaluated measuring MIC against A. baumannii. The six extracts failed to inhibit the growth of A. baumannii at the highest tested concentration (512 µg/mL) indicating that they did not have notable direct antibacterial activity against this strain at the tested concentration.
To determine the effective killing concentrations of the six extracts, the TTC reduction assay was used (Table 1). RP and GP showed the highest killing activity by having the lowest effective killing concentration (i.e., 520 µg/mL). In contrast, BR, TK, and CC showed the lowest activity by not being able to kill A. baumannii until a concentration of 640 µg/mL. Finally, CK had an intermediate value of 560 µg/mL (Table 1).
Since we could not determine a MIC value below 512 µg/mL for all six extracts, we wanted to test if they would have an impact on the growth pattern of A. baumannii. At 512 µg/ml, only BR and CC showed no significant effect on the growth curve of A. baumannii (Fig. 1A), because their curves almost overlapped with the control DMSO curve. In contrast, at this concentration all the other four extracts showed a significant delay in the time point at which the logarithmic phase started and a negative impact on the maximum extent of growth that could be reached (Fig. 1A). To confirm that this effect was only observed at high concentration, growth curve analyses of these four extracts were repeated at a lower concentration (256 µg/mL), and no impact on the growth curves was observed (Fig. 1B). It is worth mentioning, that in the case of the drug molecule orlistat, the concentration that showed no effect on bacterial growth was 64 µg/mL (data not shown). Therefore, despite the six extracts presenting negligible direct killing activity against A. baumannii, at least four of them had some effect on bacterial growth at a high concentration.
Growth curves analyses of A. baumannii in the presence of the Brassica leaf extracts. * Indicates that the difference is statistically significant as determined by the student t-test (p < 0.05, n = 3). Chinese cabbage (CC), Curly kale (CK), Tuscan kale (TK), red Pak choi (RP), green Pak choi (GP), and Brussels sprouts (BR)
Inhibitory effects against A. baumannii lipases
A. baumannii has many virulence factors, including extracellular components with hemolytic, phospholipase, protease, and iron-chelating activities, biofilm formation, surface motility, and stress resistance, which enhance its bacterial toxicity and pathogenicity [52]. While research has focused on understanding the mechanisms of antibacterial resistance, biofilm formation, and epidemiology, little is known concerning the role of secreted proteins in A. baumannii survival and propagation during infection. Targeting virulence factors with anti-virulence agents may help to prevent the development of resistance to antibiotics [53].
Lipases and phospholipases are important virulence factors of A. baumannii [52]. These enzymes degrade lipids, which are essential components of cell membranes, to facilitate nutrient acquisition, adhesion, colonization, multiplication, and invasion [54]. Lipases hydrolyze a wide range of esters, and esterolytic activity is routinely estimated by employing the pNPP assay [55]. The six extracts significantly inhibited the lipolytic activity of A. baumannii to varying extents, as shown in Fig. 2. Notably, these extract concentrations did not affect the bacterial growth itself (Fig. 1).
Remaining A. baumannii lipolytic activity after treatment with the Brassica leaf extracts for 3 h. Error bars are standard deviations of the mean, and ** and *** indicate that the p-value is < 0.01 and < 0.001 as determined by the student t-test (n = 3), respectively. Chinese cabbage (CC), Curly kale (CK), Tuscan kale (TK), red Pak choi (RP), green Pak choi (GP), Brussels sprouts (BR)
The highest activity was observed with CK with ∼ 26% inhibition at 256 µg/mL concentration, followed by both RP and GP with ∼ 21%, and TK with ∼ 15%. In contrast, BR and CC demonstrated the lowest anti-lipolytic activity with only ∼ 12.5% and ∼ 17.5% inhibition, respectively at 512 µg/mL concentration. It is worth mentioning that orlistat was shown before to bind specifically to a lipase of another species of Acinetobacter (i.e. A. radioresistens) [56]. In our hands, the orlistat inhibited the lipolytic activity by ∼ 20% at a concentration of 64 µg/mL. These findings indicated that the extracts of the investigated Brassica species would present A. baumannii lipase inhibitors, hence that they would have beneficial therapeutic activity against the infections caused by this notorious pathogen.
Multivariate data analysis
To have a better understanding of the differential metabolite distribution among the six Brassica leaf extracts and correlate the identified metabolites with the observed effects on bacterial growth and lipolytic inhibition, the complete set of 3697 compounds detected in the LC-MS metabolic profiles of the different species were subjected to unsupervised HCA and PCA, followed by supervised OPLS-DA [57].
Unsupervised HCA and PCA
HCA is an unsupervised multivariate data analysis method to explore sample heterogeneity in an intuitive graphical display called a dendrogram. HCA is an excellent tool for preliminary data analysis, where similar samples are grouped forming clusters and the distance between clusters is related to their similarity degree [58]. The HCA dendrogram (Fig. 3) shows that the six extracts were grouped into three clusters (I to III) according to their metabolic profiles. Cluster I comprised only BR and the great distance from clusters II and III, which grouped CK and TK and CC, RP, and GP, respectively, suggested important composition differences. Although HCA allows a rapid and simple preliminary data analysis, it is more informative to examine the dendrogram in conjunction with PCA.
PCA can be used to find trends and classify the different leaf extracts into different groups according to their metabolic profiles [58]. In the constructed PCA model (Fig. 4), clusters from the different extracts were located at distinct positions of the PCA score plot of the two principal components, which accounted for 31.0% (PC1) and 23.8% (PC2) of the explained variance, and no outliers were observed beyond the Hotelling’s T2 ellipse that included the 95% confidence area (Fig. 4A). In the PCA score plot (Fig. 4A), BR was clearly separated from the rest of the species along PC1, as well as along PC2 were observed three groups corresponding to CK and TK, BR and the rest of species (GP, RP, and CC). Such clustering and segregation in the PCA indicated possible chemical similarities and differences among the metabolic profiles of the studied species. Species discrimination in PCA was explained in terms of the detected compounds using the loading plot (Fig. 4B), which showed the compound contribution to the PC scores. The compounds with the largest absolute score values along each PC, which are colored in red and denoted by name in the PCA loading plot, if metabolite identity was available (Fig. 4B), were considered the most relevant to explain the three groups observed in the PCA score plot. Hydroxy oleic acid (ID 90), vanillic acid glucoside (ID 29), glucokohlrabiin (ID 4), glucoiberin (ID 2), and neoglucobrassicin (ID 15) were found to contribute the most to discriminate BR from the other species. While progoitrin (ID 3) and disinapoyl feruloyl triglucoside (ID 37) were predominated mainly in CC, RP, and GP, as well as cinnamic acid (ID 21), 4-methylpentyl glucosinolate (ID 8), 6-heptenyl glucosinolate (ID 10), and disinapoyl gentiobiose (ID 42) in TK and CK. As can be observed, glucosinolates and phenolic compounds were the main metabolites responsible for species discrimination.
Principal Component Analysis (PCA) of the Brassica leaf extracts. (A) Scores plot and (B) loading plot. The identified metabolites showing the largest absolute score values along each PC are named and colored in red and denoted by m/z and name. Chinese cabbage (CC), Curly kale (CK), Tuscan kale (TK), red Pak choi (RP), green Pak choi (GP), Brussels sprouts (BR)
Supervised OPLS-DA for metabolites-bioactivity correlation
OPLS-DA is a supervised multivariate data analysis method that can be applied to find potential specific correlations between the identified metabolites and the bioactivity results, by classifying the leaf extract samples into two groups, e.g., bioactive and non-bioactive, hence only the metabolites related to the bioactivity are influencing the groups discrimination [44, 58]. In this study, four extracts, TK, CK, RP, and GP, demonstrated significant effects on bacterial growth of A. baumannii and lipolytic activity inhibition. Therefore, a two-class OPLS-DA model was constructed with the four active extracts against the inactive extracts (CC and BR). The OPLS-DA score plot (Fig. 5A) explained 99% of the total variance (R2(X) = 0.547, R2(Y) = 0.999) with a prediction goodness parameter Q2 = 0.97 at p < 0.05. For model validation, the receiver operating characteristic (ROC) curve was calculated and the area under the curve was found to be 1.0, indicating the effectiveness of the classification model (Fig. S12A). A permutation test (20 iterations) and CV-ANOVA were conducted to evaluate whether the model was overfitted (Fig. S12B-C), with a negative Q2 intercept value and p-value < 0.05 indicating the model validity. The root mean square error of estimation (RMSEE) was 0.018 and the root mean square error of cross-validation (RMSECV) was 0.081, indicating the accuracy and the good prediction power of the model [20]. The main contributing metabolites to the bioactivities were identified in the loadings S-plot, which compared the variable magnitude against its reliability. These metabolites were further confirmed using the variable importance in the projection (VIP) and the correlation coefficient plots (Fig. 5C-D) and they are listed in detail in Table 2. As a result, nine discriminating metabolites responsible for the growth inhibitory and lipolytic effects of the active extracts (TK, CK, RP, and GP) were identified, with VIP scores > 5 and positive coefficient values (colored in red in Fig. 5C-D and listed with details in Table 2). They included one glucosinolate (ID 5), two isothiocyanates (IDs 17 and 18), four phenolic acids (IDs 21, 24, 41, and 42), and two flavonoids (IDs 51 and 59). In contrast, one organic acid (ID 68) and six fatty acids (IDs 74, 76, 79, 85, 88, and 91) were the most relevant metabolites to discriminate the inactive extracts (CC and BR) with VIP scores > 5 and negative correlation coefficients (Table 2). It is worth noting that numerous phenolic acids and flavonoids were reported to exhibit antibacterial activity against A. baumannii [59]. Several kaempferol and isorhamnetin glycosides were reported to present antibacterial and anti-virulence activities through different mechanisms, such as inhibition of sortase enzyme, biofilm formation, reduction of bacterial adhesion, and invasion [60]. It was previously reported that cinnamic and benzoic derivatives of phenolic acids (caffeic acid, gallic acid, and protocatechuic acid) are effective prooxidants with low redox potential due to their catechol rings and hydroxyl groups, thereby increasing bacterial death by triggering redox imbalance in the cells, resulting in damage to cellular macromolecules such as carbohydrates, proteins, lipids, and DNA [59]. Additionally, combining cinnamic acid with various antibiotics inhibited the expression of the biofilm-associated genes against A. baumannii [61]. Interestingly, sulforaphane and erucin were described to have antibacterial and anti-virulence activity against Pseudomonas aeruginosa, and now we found that they may possess a similar inhibition against A. baumannii [62]. Moreover, glucosinolates demonstrated antibacterial activity against a wide range of Gram-positive and Gram-negative bacteria, in addition to exerting a synergetic antibacterial effect against A. baumannii when combined with common antibiotics [63].
Orthogonal Projection on Latent Structure-Discriminant Analysis (OPLS-DA) to investigate the growth inhibitory and lipolytic effects of the Brassica leaf extracts. A two-class OPLS-DA model was constructed with the four active extracts (TK, CK, RP, and GP) against the inactive ones (CC and BR). (A) score plot, (B) loading S-plot, (C) zoomed VIP score plot, and (D) zoomed correlation coefficient plot, (Compounds contributing the most to class discrimination were colored in red and denoted by name in (B), and listed in detail in Table 2)
Molecular docking
Selected biomarkers, representatives from each class of positively correlated metabolites, including a flavonoid (brassicoside (ID 51)), a glucosinolate (glucotropaeolin (ID 5)), two phenolic acids (caffeic acid (ID 24) and cinnamic acid (ID 21)), and two isothiocyanates (sulforaphane (ID 18) and erucin (ID 17)), were subjected to molecular docking to investigate the putative interaction mechanism and predict the possible binding modes with crystallized structure of A. baumannii lipase binding site. As summarized in Table 3, all the selected metabolites exhibited interactions with lipase, displaying binding energies ranging from −70.25 to −30.20 kcal/mol. Brassicoside (ID 51) and glucotropaeolin (ID 5) presented higher binding energies compared to the reference binding ligand (i.e. orlistat, -50.13 kcal/mol). Various secondary interactions, such as hydrogen bonding, hydrophobic, and aromatic stacking interactions, were raised between the selected metabolites and different amino acid residues of the crystallized structure of the A. baumannii lipase receptor. These interactions likely contributed to the observed inhibitory effect of the selected metabolites.
The predicted binding mode for orlistat displayed that both oxygen atoms and the attached carbonyl group at the 2-position of oxetane were involved in a hydrogen bonding interaction with Arg260. Furthermore, the carbonyl group of formamide moiety participated in a water-mediated interaction with the backbone carbonyl group of Ala126. Additionally, the carbonyl group of orlistat formed another hydrogen bond with Ser257. In terms of hydrophobic interactions, the hexyl moiety of orlistat predominantly occupied the hydrophobic pocket formed by Ala79, Trp114, Leu129, Trp166, and Leu167, while the tridecane showed hydrophobic interactions with Leu110, Phe111, Trp220, and Trp222. In contrast, the isopentane moiety was engaged in an unfavorable interaction with Glu113. Consequently, hydrophilic residues played essential roles in the binding of orlistat to the crystallized structure of A. baumannii lipase receptor (Fig. 6a).
The predicted binding mode for brassicoside (ID 51) revealed that its polyphenolic moieties were oriented to the enzyme active site, engaging in hydrogen bonding interactions with the backbone amino groups of Trp220, Ser257, Ser258, and Arg260. Additionally, the phenolic groups participated in hydrogen bonding interactions with the backbone carbonyl groups of Ala126, Trp220, and Trp222, along with aromatic stacking interactions with Phe111, Trp114, and Trp220. Additionally, these groups were involved in hydrophobic interactions primarily with Leu110, Leu129, and Leu167. Figure 6b presents the docked metabolite inside the binding pocket. The predicted binding mode for glucotropaeolin (ID 5) suggested that the dihydroxy groups of the pyran moiety were involved in hydrogen bonding and water-mediated interactions with Glu113. In addition, the benzyl moiety was stabilized through aromatic stacking interactions with Phe111, Trp114, Trp220, and Trp222, and was located in the hydrophobic pocket formed by Ala79, Leu129, and Leu167. On the other hand, the sulfonic moiety was surrounded by hydrogen bonding interactions with Arg260, and water-mediated interactions with Lys125, Ser127, and Ser218, which formed a pocket that contributed to an enhanced affinity of glucotropaeolin with the binding site (Fig. 6c). Furthermore, the molecular docking result for caffeic acid (ID 24) demonstrated that the carboxylic moiety was anchored by a hydrogen bonding interaction with the gatekeeper residue, Ser257. Additionally, the styrene moiety was located in hydrophobic interactions with Ala79, Leu110, Leu129, and Leu167, and formed aromatic stacking interactions with Phe111, Trp114, Trp220, and Trp222. Finally, its hydroxyl group was located at a distance of 2.7 Å from Ser80 (Table 3, Fig. S13a). On the other hand, the binding mode of cinnamic acid (ID 21) was similar to that of caffeic acid (ID 24) with an affinity value of -40.99 kcal/mol. In this case, its carboxylic and styrene moieties maintained the same hydrogen bonding, hydrophobic, and aromatic stacking interactions. However, the favorable interaction of hydroxyl moiety with Ser80 was abolished, which may explain its lower affinity compared with caffeic acid (ID 24) (Table 3, Fig. S13b).
Additionally, the proposed binding mode of sulforaphane (ID 18) with the crystal structure of A. baumannii lipase indicated that the sulfinyl group formed hydrogen bonding interactions with Arg260, while the butane moiety was involved in hydrophobic interactions with Leu110, Phe111, Trp114, Trp220, and Trp222. The binding mode of erucin (ID 17) was similar to sulforaphane however, the hydrogen bonding interaction with Arg260 was annulled (Table 3, Fig. S13c). Overall, an examination of the interacting amino acid residues in Table 3 revealed consistent binding modes among all selected metabolites, with brassicoside (ID 51) and glucotropaeolin (ID 5) exhibiting more extensive interactions across all three types of interactions, similar to orlistat. Upon analyzing the favorable binding poses, four essential hydrogen bonding interactions were identified, involving Glu113, Ser257, Ser258, and Arg260 residues. Additionally, the contributions of aromatic stacking resulted from a more deeply located binding pose within the binding site of the A. baumannii receptor. These hydrogen bonding interactions, along with aromatic stacking interactions, particularly with aromatic amino acid residues Phe111, Trp114, Trp220, and Trp222, appeared to be pivotal factors contributing to the higher affinity of brassicoside and glucotropaeolin towards the A. baumannii receptor, playing a significant role in bacterial lipase inhibition.
Conclusions
In conclusion, our results are promising and support the use of Brassica leaf extracts as novel sources of natural antibacterial and anti-virulence agents for multi-drug resistant bacteria. Notably, extracts from TK, CK, RP, and GP exhibited the most substantial profiles of bioactive metabolites. Among these bioactive metabolites, the flavonoid brassicoside and the glucosinolate glucotropaeolin displayed the highest potential for inhibiting the A. baumannii lipase enzyme. This discovery holds significance not only for pharmaceutical applications but also for the development of novel breeding programs focused on Brassica vegetables as functional foods and valuable sources of nutraceuticals.
Data availability
The data supporting the findings of this study are available within the article and its supplementary file.
Abbreviations
- CV-ANOVA:
-
cross-validated analysis of variance
- HCA:
-
Hierarchical cluster analysis
- LC-QTOF-MS/MS:
-
liquid chromatography-quadrupole time-of-flight tandem mass spectrometry
- PCA:
-
principal component analysis
- RMSEcv:
-
root mean square of error of cross-validation
- RMSEE:
-
root mean square error of estimation
- ROC:
-
receiver operating characteristic
- VIP:
-
variable importance to projection
References
Kapusta-Duch J, Kopec A, Piatkowska E, Borczak B, Leszczynska T. The beneficial effects of Brassica vegetables on human health. Roczniki Państwowego Zakładu Higieny 2012, 63(4).
Jaiswal AK, Abu-Ghannam N, Gupta S. A comparative study on the polyphenolic content, antibacterial activity and antioxidant capacity of different solvent extracts of Brassica oleracea vegetables. Int J Food Sci Technol. 2012;47(2):223–31.
Ayaz FA, Hayırlıoglu-Ayaz S, Alpay-Karaoglu S, Grúz J, Valentová K, Ulrichová J, Strnad M. Phenolic acid contents of kale (Brassica Oleraceae L. var. Acephala DC.) Extracts and their antioxidant and antibacterial activities. Food Chem. 2008;107(1):19–25.
Lim H-W, Song K-Y, Chon J-W, Jeong D, Seo K-H. Antimicrobial action of Raphanus raphanistrum subsp. sativus (radish) extracts against foodborne bacteria present in various milk products: a preliminary study. J Dairy Sci Biotechnol. 2019;37(3):187–95.
Hu SH, Wang JC, Kung HF, Wang JT, Lee WL, Yang YH. Antimicrobial effect of extracts of cruciferous vegetables. Kaohsiung J Med Sci. 2004;20(12):591–9.
Bell L, Kitsopanou E, Oloyede OO, Lignou S. Important odorants of four Brassicaceae species, and discrepancies between glucosinolate profiles and observed hydrolysis products. Foods. 2021;10(5):1055.
Prieto M, López CJ, Simal-Gandara J. Glucosinolates: molecular structure, breakdown, genetic, bioavailability, properties and healthy and adverse effects. Adv Food Nutr Res. 2019;90:305–50.
Sun J, Xiao Z, Lin L-z, Lester GE, Wang Q, Harnly JM, Chen P. Profiling polyphenols in five Brassica species microgreens by UHPLC-PDA-ESI/HRMSn. J Agric Food Chem. 2013;61(46):10960–70.
Satish A, Farha SS, Urooj A. Quantification of flavonoids by UPLC-MS and its antibacterial activity from Brassica oleracea var. Capitata L. GSC Biol Pharm Sci. 2018;5(1):109–14.
Lin L-Z, Harnly JM. Identification of the phenolic components of collard greens, kale, and Chinese broccoli. J Agric Food Chem. 2009;57(16):7401–8.
Sharma I, Aaradhya M, Kodikonda M, Naik PR. Antihyperglycemic, antihyperlipidemic and antioxidant activity of phenolic rich extract of Brassica oleraceae var gongylodes on streptozotocin induced Wistar rats. Springerplus. 2015;4(1):1–7.
Khalil MN, Afifi SM, Eltanany BM, Pont L, Benavente F, El-Sonbaty SM, Sedeek MS. Assessment of the effect of drying on Brassica greens via a multiplex approach based on LC-QTOF-MS/MS, molecular networking, and chemometrics along with their antioxidant and anticancer activities. Food Res Int 2024:114053.
Khalil HE, Abdelwahab MF, Emeka PM, Badger-Emeka LI, Ahmed A-SF, Anter AF, Abdel Hafez SMN, AlYahya KA, Ibrahim H-IM, Thirugnanasambantham K. Brassica oleracea L. Var. botrytis leaf extract alleviates gentamicin-induced hepatorenal injury in rats—possible modulation of IL-1β and NF-κB activity assisted with computational approach. Life. 2022;12(9):1370.
Khalil HE, Abdelwahab MF, Emeka PM, Badger-Emeka LI, Abdel Hafez SMN, AlYahya KA, Ahmed A-SF, Anter AF, Abdel-Wahab NM, Matsunami K. Chemical composition and valorization of broccoli Leaf by-products (Brassica oleracea L. variety: italica) to ameliorate reno-hepatic toxicity induced by gentamicin in rats. Appl Sci. 2022;12(14):6903.
Aires A, Mota V, Saavedra M, Rosa E, Bennett R. The antimicrobial effects of glucosinolates and their respective enzymatic hydrolysis products on bacteria isolated from the human intestinal tract. J Appl Microbiol. 2009;106(6):2086–95.
Borges A, Abreu AC, Ferreira C, Saavedra MJ, Simões LC, Simões M. Antibacterial activity and mode of action of selected glucosinolate hydrolysis products against bacterial pathogens. J Food Sci Technol. 2015;52:4737–48.
Jang M, Hong E, Kim GH. Evaluation of antibacterial activity of 3-butenyl, 4‐pentenyl, 2‐phenylethyl, and benzyl isothiocyanate in Brassica vegetables. J Food Sci. 2010;75(7):M412–6.
Liu J, Liu Y, Wang Y, Abozeid A, Zu Y-G, Tang Z-H. The integration of GC–MS and LC–MS to assay the metabolomics profiling in Panax ginseng and Panax quinquefolius reveals a tissue-and species-specific connectivity of primary metabolites and ginsenosides accumulation. J Pharm Biomed Anal. 2017;135:176–85.
Farag MA, Kabbash EM, Mediani A, Döll S, Esatbeyoglu T, Afifi SM. Comparative metabolite fingerprinting of four different cinnamon species analyzed via UPLC–MS and GC–MS and chemometric tools. Molecules. 2022;27(9):2935.
Ibrahim RM, Eltanany BM, Pont L, Benavente F, ElBanna SA, Otify AM. Unveiling the functional components and antivirulence activity of mustard leaves using an LC-MS/MS, molecular networking, and multivariate data analysis integrated approach. Food Res Int. 2023;168:112742.
Ibrahim RM, Fayez S, Eltanany BM, Abu-Elghait M, El-Demerdash A, Badawy MSE, Pont L, Benavente F, Saber FR. Agro-byproduct valorization of radish and turnip leaves and roots as new sources of antibacterial and antivirulence agents through metabolomics and molecular networking. Sci Hort. 2024;328:112924.
Harbaum B, Hubbermann EM, Wolff C, Herges R, Zhu Z, Schwarz K. Identification of flavonoids and hydroxycinnamic acids in Pak Choi varieties (Brassica campestris L. ssp. chinensis var. Communis) by HPLC–ESI-MSn and NMR and their quantification by HPLC–DAD. J Agric Food Chem. 2007;55(20):8251–60.
Matthäus B, Luftmann H. Glucosinolates in members of the family Brassicaceae: separation and identification by LC/ESI-MS-MS. J Agric Food Chem. 2000;48(6):2234–9.
Wu W, Chen J, Yu D, Chen S, Ye X, Zhang Z. Analysis of processing effects on glucosinolate profiles in red cabbage by LC-MS/MS in multiple reaction monitoring mode. Molecules. 2021;26(17):5171.
Sasaki K, Neyazaki M, Shindo K, Ogawa T, Momose M. Quantitative profiling of glucosinolates by LC–MS analysis reveals several cultivars of cabbage and kale as promising sources of sulforaphane. J Chromatogr B. 2012;903:171–6.
Rizk SS, Elwakil WH, Attia AS. Antibiotic-resistant Acinetobacter baumannii in low-income countries (2000–2020): twenty-one years and still below the radar, is it not there or can they not afford to look for it? Antibiotics. 2021;10(7):764.
World Health Organization W: Cad Pesqui. 2017, 43:348–365.
Lee C-R, Lee JH, Park M, Park KS, Bae IK, Kim YB, Cha C-J, Jeong BC, Lee SH. Biology of Acinetobacter baumannii: pathogenesis, antibiotic resistance mechanisms, and prospective treatment options. Front Cell Infect Microbiol. 2017;7:55.
Sabry MM, Abdel-Rahman RF, Fayed HM, Taher AT, Ogaly HA, Albohy A, El-Gayed SH, Ibrahim RM. Impact of Eucalyptus maculata hook resin exudate constituents on reducing COX-2 gene expression: In-vivo anti-inflammatory, molecular docking and dynamics studies. J Ethnopharmacol. 2023;314:116631.
Asiamah I, Obiri SA, Tamekloe W, Armah FA, Borquaye LS. Applications of molecular docking in natural products-based drug discovery. Sci Afr 2023:e01593.
Alruwad MI, Sabry MM, Gendy AM, El-Dine RS, El Hefnawy HM. In vitro cytotoxic potential of selected Jordanian flora and their associated phytochemical analysis. Plants. 2023;12:1626.
Pluskal T, Castillo S, Villar-Briones A, Orešič M. MZmine 2: modular framework for processing, visualizing, and analyzing mass spectrometry-based molecular profile data. BMC Bioinformatics. 2010;11(1):1–11.
Elhosseiny NM, Elhezawy NB, Attia AS. Comparative proteomics analyses of Acinetobacter baumannii strains ATCC 17978 and AB5075 reveal the differential role of type II secretion system secretomes in lung colonization and ciprofloxacin resistance. Microb Pathog. 2019;128:20–7.
CLSI C. Performance standards for antimicrobial susceptibility testing. Clin Lab Standard Inst. 2016;35:16–38.
Eloff JN. A sensitive and quick microplate method to determine the minimal inhibitory concentration of plant extracts for bacteria. Planta Med. 1998;64:711–3.
Elhosseiny NM, Amin MA, Yassin AS, Attia AS. Acinetobacter Baumannii universal stress protein A plays a pivotal role in stress response and is essential for pneumonia and sepsis pathogenesis. Int J Med Microbiol. 2015;305:114–23.
Martinez-Corona R, Banderas-Martinez FJ, Perez-Castillo JN, Cortes-Penagos C, Gonzalez-Hernandez JC. Avocado oil as an inducer of the extracellular lipase activity of Kluyveromyces marxianus L-2029. Food Sci Technol. 2019;40:121–9.
Morris GM, Goodsell DS, Halliday RS, Huey R, Hart WE, Belew RK, Olson AJ. Automated docking using a lamarckian genetic algorithm and an empirical binding free energy function. J Comput Chem. 1998;19(14):1639–62.
Hooshmand K, Fomsgaard IS. Analytical methods for quantification and identification of intact glucosinolates in Arabidopsis roots using LC-QqQ (LIT)-MS/MS. Metabolites. 2021;11(1):47.
Grubb CD, Abel S. Glucosinolate metabolism and its control. Trends Plant Sci. 2006;11(2):89–100.
Sikorska-Zimny K, Beneduce L. The glucosinolates and their bioactive derivatives in Brassica: a review on classification, biosynthesis and content in plant tissues, fate during and after processing, effect on the human organism and interaction with the gut microbiota. Crit Rev Food Sci Nutr. 2021;61(15):2544–71.
Ishihara S, Inaoka T, Nakamura T, Kimura K, Sekiyama Y, Tomita S. Nuclear magnetic resonance-and gas chromatography/mass spectrometry-based metabolomic characterization of water-soluble and volatile compound profiles in cabbage vinegar. J Biosci Bioeng. 2018;126(1):53–62.
Kolodiazhna AО, Skliarov АI, Slastennikova AA, Kolodiazhnyi OI. Asymmetric synthesis of (S, R)-and (R, R)-methiin stereoisomers. Phosphorus Sulfur Silicon Relat Elem. 2020;195(9):713–7.
Han D, Row KH. Separation and purification of sulforaphane from broccoli by solid phase extraction. Int J Mol Sci. 2011;12(3):1854–61.
Matusheski NV, Jeffery EH. Comparison of the bioactivity of two glucoraphanin hydrolysis products found in broccoli, sulforaphane and sulforaphane nitrile. J Agric Food Chem. 2001;49(12):5743–9.
Rose P, Huang Q, Ong CN, Whiteman M. Broccoli and watercress suppress matrix metalloproteinase-9 activity and invasiveness of human MDA-MB-231 breast cancer cells. Toxicol Appl Pharmcol. 2005;209(2):105–13.
Sun J, Liang F, Bin Y, Li P, Duan C. Screening non-colored phenolics in red wines using liquid chromatography/ultraviolet and mass spectrometry/mass spectrometry libraries. Molecules. 2007;12(3):679–93.
Lin L-Z, Harnly JM. Phenolic component profiles of mustard greens, Yu Choy, and 15 other Brassica vegetables. J Agric Food Chem. 2010;58(11):6850–7.
Ferreres F, Sousa C, Vrchovská V, Valentão P, Pereira JA, Seabra RM, Andrade PB. Chemical composition and antioxidant activity of tronchuda cabbage internal leaves. Eur Food Res Technol. 2006;222:88–98.
Cartea ME, Francisco M, Soengas P, Velasco P. Phenolic compounds in Brassica vegetables. Molecules. 2010;16(1):251–80.
Sharafi Y, Majidi MM, Goli SAH, Rashidi F. Oil content and fatty acids composition in Brassica species. Int J Food Prop. 2015;18(10):2145–54.
Elhosseiny NM, El-Tayeb OM, Yassin AS, Lory S, Attia AS. The secretome of Acinetobacter baumannii ATCC 17978 type II secretion system reveals a novel plasmid encoded phospholipase that could be implicated in lung colonization. Int J Med Microbiol. 2016;306(8):633–41.
Fleitas Martínez O, Cardoso MH, Ribeiro SM, Franco OL. Recent advances in anti-virulence therapeutic strategies with a focus on dismantling bacterial membrane microdomains, toxin neutralization, quorum-sensing interference and biofilm inhibition. Front Cell Infect Microbiol. 2019;9:74.
Johnson TL, Waack U, Smith S, Mobley H, Sandkvist M. Acinetobacter baumannii is dependent on the type II secretion system and its substrate LipA for lipid utilization and in vivo fitness. J Bacteriol. 2016;198(4):711–9.
Snellman EA, Sullivan ER, Colwell RR. Purification and properties of the extracellular lipase, LipA, of Acinetobacter sp. RAG-1. Eur J Biochem. 2002;269(23):5771–9.
Gupta KK, Mandal R, Jagtap S, Ramadas K. Glucovanillin: a potent inhibitor of lipase from Acinetobacter radioresistens. Inf Med Unlocked. 2018;10:126–33.
Madala NE, Piater LA, Steenkamp PA, Dubery IA. Multivariate statistical models of metabolomic data reveals different metabolite distribution patterns in isonitrosoacetophenone-elicited Nicotiana tabacum and Sorghum bicolor cells. SpringerPlus. 2014;3(1):1–10.
Betancur LA, Naranjo-Gaybor SJ, Vinchira-Villarraga DM, Moreno-Sarmiento NC, Maldonado LA, Suarez-Moreno ZR, Acosta-González A, Padilla-Gonzalez GF, Puyana M, Castellanos L. Marine Actinobacteria as a source of compounds for phytopathogen control: an integrative metabolic-profiling/bioactivity and taxonomical approach. PLoS ONE. 2017;12(2):e0170148.
Ajiboye TO, Skiebe E, Wilharm G. Phenolic acids potentiate colistin-mediated killing of Acinetobacter baumannii by inducing redox imbalance. Biomed Pharmacother. 2018;101:737–44.
Abdelaziz NA, Elkhatib WF, Sherif MM, Abourehab MA, Al-Rashood ST, Eldehna WM, Mostafa NM, Elleboudy NS. In silico docking, resistance modulation and biofilm gene expression in multidrug-resistant Acinetobacter baumannii via cinnamic and gallic acids. Antibiotics. 2022;11(7):870.
Nitulescu G, Margina D, Zanfirescu A, Olaru OT, Nitulescu GM. Targeting bacterial sortases in search of anti-virulence therapies with low risk of resistance development. Pharmaceuticals. 2021;14(5):415.
Ganin H, Rayo J, Amara N, Levy N, Krief P, Meijler MM. Sulforaphane and erucin, natural isothiocyanates from broccoli, inhibit bacterial quorum sensing. RSC Med Chem. 2013;4(1):175–9.
Frank U, Ngalah BS, Börner K, Finkbeiner J, Harter A, Biehler K. Combination of isothiocyanates and antibiotics increases susceptibility against Acinetobacter Baumannii, Escherichia Coli, Klebsiella Pneumoniae, Proteus Mirabilis and Serratia Marcescens. Escherichia Coli, Klebsiella Pneumoniae, Proteus Mirabilis and Serratia Marcescens.
Acknowledgements
Basma M. Eltanany would like to thank the Egyptian Ministry of Higher Education for funding her postdoctoral research stay with the Bioanalysis group at the University of Barcelona (UB), Barcelona, Spain. The Bioanalysis group of the UB is part of the INSA-UB Maria de Maeztu Unit of Excellence (Grant CEX2021-001234-M) funded by MICIN/AEI/FEDER, UE.
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Open access funding provided by The Science, Technology & Innovation Funding Authority (STDF) in cooperation with The Egyptian Knowledge Bank (EKB).
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M.M.S.; Conceptualization, Supervision, Writing original draft. A.M.E.; Methodology, W.G.F., Methodology, Writing – Review and Editing, B.M.E., and L.P.; Data curation, Investigation, Methodology, Writing - Review and Editing, F.B.; Supervision, Writing - Review and Editing, A.S.A.; Methodology, Writing – Review and Editing, F.F.S.; Investigation, Methodology, Formal analysis, Writing - Review and Editing, R.M.I.; Conceptualization, Investigation, Methodology, Formal analysis, Data curation, Writing original draft. All authors reviewed the manuscript.
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Sabry, M.M., El-Halawany, A.M., Fahmy, W.G. et al. Evidence on the inhibitory effect of Brassica plants against Acinetobacter baumannii lipases: phytochemical analysis, in vitro, and molecular docking studies. BMC Complement Med Ther 24, 164 (2024). https://doi.org/10.1186/s12906-024-04460-y
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DOI: https://doi.org/10.1186/s12906-024-04460-y